← Back to all trials
Not Yet Recruiting
NCT05713136
The National Australian HCV Point-of-Care Testing Program - HCV Antibody Testing Minimal Dataset
Conditions: Hepatitis C
Sex: All
Ages: 18 Years – N/A
Healthy volunteers: 1
Enrollment: 40000
Sponsor: Kirby Institute
Summary
This is an observational cohort study.
Participants will be recruited from settings that provide services to people with a risk factor for the acquisition of HCV infection.
Participants will attend a single visit to have HCV point-of-care testing.
Participants who have not previously received HCV treatment will have a point-of-care HCV antibody test, followed by reflex point-of-care HCV RNA test if positive.
Those who have a history of HCV treatment will proceed straight to point-of-care HCV RNA testing.
Participants will not receive treatment as a part of this study.
Participants who are HCV RNA positive will receive treatment via standard of care.
The purpose of this study is to look at the effect of finger-stick point-of-care hepatitis C testing, to see if it increases the number of tests, diagnoses, and treatments for people with a risk factor of having hepatitis C in Australia.
Eligibility Criteria
Inclusion Criteria:Provide informed consent≥ 18 years of age.Exclusion Criteria:Is unable or unwilling to provide informed consent
Source: ClinicalTrials.gov (NCT05713136). StuddyBuddy aggregates publicly available trial information.